Molecular and Genetic Markers for Malignant Melanoma: Implications for Prognosis and Therapy.

IF 1.7 Q3 DERMATOLOGY
Lauren Fleshner, Alyssa Sayegh, Mehmet Fatih Atak, Rahim Hirani, Banu Farabi, Bijan Safai, Shoshana Marmon
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引用次数: 0

Abstract

Despite therapeutic advancements, malignant melanoma remains a leading cause of skin cancer-related mortality, with incidence continuing to rise globally. Traditional prognostic tools offer important clinical guidance but fail to capture the biological heterogeneity of melanoma or reliably predict responses to emerging therapies. In this review, we summarize recent advances in prognostic and predictive molecular biomarkers reported over the past five years. We discuss immunohistochemical and tissue-based markers, circulating biomarkers, microRNAs, and gene expression profiles that enhance risk stratification and inform surveillance strategies. We also review immune-related markers that may predict response to immune-checkpoint inhibitor therapy. Lastly, we highlight investigational biomarkers-including gene signatures, epigenomic alterations, and microbiome influences-that are shaping the future landscape. Together, these advances reflect a shift toward precision oncology in melanoma, with the integration of biomarker-driven strategies offering the potential to personalize treatment and improve patient outcomes.

恶性黑色素瘤的分子和遗传标记:对预后和治疗的影响。
尽管治疗取得了进步,但恶性黑色素瘤仍然是皮肤癌相关死亡的主要原因,全球发病率持续上升。传统的预后工具提供了重要的临床指导,但未能捕捉黑色素瘤的生物学异质性或可靠地预测对新兴疗法的反应。在这篇综述中,我们总结了近五年来预后和预测分子生物标志物的最新进展。我们讨论了免疫组织化学和基于组织的标志物、循环生物标志物、microrna和基因表达谱,它们可以增强风险分层并为监测策略提供信息。我们还回顾了可能预测免疫检查点抑制剂治疗反应的免疫相关标志物。最后,我们强调了正在塑造未来景观的研究性生物标志物,包括基因特征、表观基因组改变和微生物组影响。总之,这些进展反映了黑色素瘤向精确肿瘤学的转变,生物标志物驱动策略的整合提供了个性化治疗和改善患者预后的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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